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PEX1 Produits

(Peroxisomal Biogenesis Factor 1 (PEX1))

Catégories

This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities.

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Catégories PEX1 en vedette

PEX1 Anticorps

High quality antibodies with extensive validation data.

PEX1 Protéines

Proteins for various applications incl. WB, ELISA, IF etc.

PEX1 recommandé Anticorps

Produit
Reactivity
Application
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human
Application ICC, IHC, WB
Validations
  • collections(3)
N° du produit ABIN5014081
Quantité 100 μL
Reactivity Mouse
Application ICC, IHC, WB
Validations
  • collections(3)
N° du produit ABIN5014080
Quantité 100 μL
Reactivity Mouse, Rat
Application ELISA, WB
Validations
  • collections(1)
N° du produit ABIN570873
Quantité 100 μg

PEX1 recommandé Kits ELISA

Produit
Reactivity
Analytical Method
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human
Analytical Method Sandwich ELISA
Validations
N° du produit ABIN418397
Quantité 96 tests

PEX1 recommandé Protéines

Produit
Reactivity
Source
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human
Source Insect Cells
Validations
  • collections(1)
N° du produit ABIN3094488
Quantité 1 mg
Reactivity Mouse
Source Insect Cells
Validations
  • collections(1)
N° du produit ABIN3135168
Quantité 1 mg
Reactivity Human
Source Escherichia coli (E. coli)
Validations
N° du produit ABIN7086927
Quantité 50 μg

Dernières publications sur nos produits PEX1

Pedrosa, Francisco, Bicho, Dias, Barros-Barbosa, Hagmann, Dodt, Rodrigues, Azevedo: "Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol." dans: The Journal of biological chemistry, Vol. 293, Issue 29, pp. 11553-11563, (2019) (PubMed).

Yik, Steinberg, Moser, Moser, Hacia: "Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders." dans: Human mutation, Vol. 30, Issue 3, pp. E467-80, (2009) (PubMed).

Collins, Gould: "Identification of a common PEX1 mutation in Zellweger syndrome." dans: Human mutation, Vol. 14, Issue 1, pp. 45-53, (1999) (PubMed).

Geisbrecht, Collins, Reuber, Gould: "Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, Issue 15, pp. 8630-5, (1998) (PubMed).

Reuber, Germain-Lee, Collins, Morrell, Ameritunga, Moser, Valle, Gould: "Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders." dans: Nature genetics, Vol. 17, Issue 4, pp. 445-8, (1997) (PubMed).

Synonymes et noms alternatifs relatifs à PEX1

peroxisomal biogenesis factor 1 (PEX1), peroxisomal biogenesis factor 1 (Pex1), peroxisomal biogenesis factor 1 L homeolog (pex1.L), 5430414H02Rik, E330005K07Rik, PBD1A, PBD1B, pex1, RGD1559939, ZWS, ZWS1

Protein level used designations for PEX1

  • Zellweger syndrome
  • peroxin-1
  • peroxisome biogenesis disorder protein 1
  • peroxisome biogenesis factor 1
  • peroxisomal biogenesis factor 1 L homeolog
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